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"68001-322-04" National Drug Code (NDC)

Bupropion Hydrochloride 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68001-322-04)
(BluePoint Laboratories)

NDC Code68001-322-04
Package Description30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68001-322-04)
Product NDC68001-322
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Proprietary Name Suffix(xl)
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20170322
End Marketing Date20221130
Marketing Category NameANDA
Application NumberANDA206556
ManufacturerBluePoint Laboratories
Substance NameBUPROPION HYDROCHLORIDE
Strength150
Strength Unitmg/1
Pharmacy ClassesAminoketone [EPC], Dopamine Uptake Inhibitors [MoA], Increased Dopamine Activity [PE], Increased Norepinephrine Activity [PE], Norepinephrine Uptake Inhibitors [MoA]

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